Reginald H. Mitchell, Thottumkara K. Vinod, Gordon W. Bushnell. syn-[2.2]Metacyclophane: isolation, NMR properties and facile isomerization to anti-[2.2]metacyclophane. A synthesis involving bridge reactions of chromium tricarbonyl complexed dithiametacyclophanes. „J. Am. Chem. Soc.”. 112 (9), s. 3487–3497, 1990. DOI: 10.1021/ja00165a037.
Paulo F. T. Schirch, Virgil Boekelheide. [2.2.2.2.2](1,2,3,4,5)Cyclophane. „J. Am. Chem. Soc.”. 101 (11), s. 3126–3127, 1979. DOI: 10.1021/ja00505a052.
Yasuo Sekine, V. BoekelheideA study of the synthesis and properties of [26](1,2,3,4,5,6)cyclophane (superphane). „J. Am. Chem. Soc.”. 103 (7), s. 1777–1785, 1981. DOI: 10.1021/ja00397a032.
Robert A. Pascal, Jr. Molecular „Iron Maidens”: Ultrashort Nonbonded Contacts in Cyclophanes and Other Crowded Molecules. „Eur. J. Org. Chem.”, s. 3763–3771, 2004. DOI: 10.1002/ejoc.200400183.
Robert A. Pascal Jr., Robert B. Grossman, Donna Van Engen. Synthesis of in-[34,10][7]metacyclophane: projection of an aliphatic hydrogen toward the center of an aromatic ring. „J. Am. Chem. Soc.”. 109 (22), s. 6878–6880, 1987. DOI: 10.1021/ja00256a067.